Canonical Allele Identifier: CA2652424154

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32808170-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808170T>C , CM000682.2:g.32808170T>C	GRCh38
NC_000020.10:g.31395976T>C , CM000682.1:g.31395976T>C	GRCh37
NC_000020.9:g.30859637T>C	NCBI36
NG_007290.1:g.50786T>C , LRG_56:g.50786T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1780T>C	ENSP00000512497.1:n.*1780T>C
ENST00000696232.1:c.*267T>C	ENSP00000512498.1:n.*267T>C
ENST00000696233.1:c.*1383T>C	ENSP00000512499.1:n.*1383T>C
ENST00000696238.1:c.*1572T>C	ENSP00000512502.1:n.*1572T>C
ENST00000696245.1:n.854T>C
ENST00000201963.3:c.*267T>C	ENSP00000201963.3:n.*267T>C
ENST00000328111.6:c.*267T>C MANE Select	ENSP00000328547.2:n.*267T>C
ENST00000348286.6:c.*267T>C	ENSP00000337764.2:n.*267T>C
ENST00000353855.6:c.*267T>C	ENSP00000313397.4:n.*267T>C
ENST00000443239.7:c.*267T>C	ENSP00000403169.2:n.*267T>C
NM_001207055.1:c.*267T>C	NP_001193984.1:n.*267T>C
NM_001207056.1:c.*267T>C	NP_001193985.1:n.*267T>C
NM_006892.3:c.*267T>C , LRG_56t1:c.*267T>C	NP_008823.1:n.*267T>C
NM_175848.1:c.*267T>C	NP_787044.1:n.*267T>C
NM_175849.1:c.*267T>C	NP_787045.1:n.*267T>C
NM_175850.2:c.*267T>C	NP_787046.1:n.*267T>C
XM_011528653.1:c.*267T>C	XP_011526955.1:n.*267T>C
XM_011528654.1:c.*267T>C	XP_011526956.1:n.*267T>C
XR_936511.1:n.2607T>C
XM_011528653.2:c.*267T>C	XP_011526955.1:n.*267T>C
XM_011528654.2:c.*267T>C	XP_011526956.1:n.*267T>C
XR_936511.2:n.2618T>C
NM_001207055.2:c.*267T>C	NP_001193984.1:n.*267T>C
NM_001207056.2:c.*267T>C	NP_001193985.1:n.*267T>C
NM_006892.4:c.*267T>C MANE Select	NP_008823.1:n.*267T>C
NM_175848.2:c.*267T>C	NP_787044.1:n.*267T>C
NM_175849.2:c.*267T>C	NP_787045.1:n.*267T>C
NM_175850.3:c.*267T>C	NP_787046.1:n.*267T>C